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<?xml-stylesheet type="text/xsl" href="https://community.macmillan.org.uk/cfs-file/__key/system/syndication/atom.xsl" media="screen"?><feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en-US"><title type="html">emmaemily34&amp;#39;s blog </title><subtitle type="html">emmaemily34&amp;#39;s blog </subtitle><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2009-10-17T10:34:45Z</updated><entry><title>Stress</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/stress" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/stress</id><published>2011-01-07T18:43:29Z</published><updated>2011-01-07T18:43:29Z</updated><content type="html">&lt;p&gt;Been signed off work due to stress, seems beating Cancer was just the start, three bouts of Cellulites which has me in hospital each time. Being a single mum is just so hard!!&amp;nbsp;&amp;nbsp;&amp;nbsp; it just seems unfair went through all that now this when will it end?? Grrrrrrrrr !&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=394520&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Hospital" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/Hospital" /></entry><entry><title>Cellulitis</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/cellulitis" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/cellulitis</id><published>2010-04-24T10:14:29Z</published><updated>2010-04-24T10:14:29Z</updated><content type="html">&lt;p&gt;Last Saturday woke up feeling fine but within an hour had the horrible shakes and the odd feeling which i recognise has a high temperature trying frantically to fine my themonitor which i was told to always keep handy but after a frantic search could not find, phoning nhs help line have to say not much help, and feeling more and more poorly only having my youngest son here tried to phone my team at addenbrookes then i remembered the purple card with my ward number so phoned them and they said phone an ambulance which i did and 20 mins later two men came to my rescue got me in ambulance and temp was 39.7 got to hospital turns out it was cellulitis which i had not even heard of, so the iv was put in and 63 hours of antibiotics was in, home Tuesday and today still feeling weak have a check up on Tuesday what an ordeal just goes to show never let your guard down, and thank goodness i phoned for that ambulance and not make a cup of tea has told by the person on the helpline!&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=333417&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Hospital" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/Hospital" /><category term="temperature" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/temperature" /></entry><entry><title>Its clear!!!</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/its-clear" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/its-clear</id><published>2010-02-17T09:21:28Z</published><updated>2010-02-17T09:21:28Z</updated><content type="html">&lt;p&gt;My specialist nurse phoned me up to say no need to make the journey in has results have come back clear!&amp;nbsp; What an amazing feeling i just wish all of you amazing people could feel it&lt;/p&gt;
&lt;p&gt;Love to you all&amp;nbsp; x x x x&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=317069&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author></entry><entry><title>Has it come back?</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/has-it-come-back" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/has-it-come-back</id><published>2010-02-12T13:03:18Z</published><updated>2010-02-12T13:03:18Z</updated><content type="html">&lt;p&gt;Oh dear, &lt;/p&gt;
&lt;p&gt;went to Addenbrookes to see my Dr Gorgeous has i had another sore patch so had a biopsy taken will get results on Wednesday.&amp;nbsp; But things feel different this time around, not terrified,not upset perhaps a little numb about it all, No way am i going to let it scare me has much has it did last time,Beat it once i can beat it again .&amp;nbsp; So once again its the waiting game, will let you guys know has soon has i know&lt;/p&gt;
&lt;p&gt;xxxx&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=315825&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="biopsy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/biopsy" /></entry><entry><title>Race for Life</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/race-for-life" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/race-for-life</id><published>2010-01-15T17:05:04Z</published><updated>2010-01-15T17:05:04Z</updated><content type="html">&lt;p&gt;&lt;span&gt;www.raceforlifesponsorme.org/emmaflanaga&lt;/span&gt;&lt;span class="word_break"&gt;&lt;/span&gt;n1&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=308116&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author></entry><entry><title>best news ever</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/best-news-ever" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/best-news-ever</id><published>2009-12-21T10:32:26Z</published><updated>2009-12-21T10:32:26Z</updated><content type="html">&lt;p&gt;21/12/09&amp;nbsp; this day i will remember for ever!&amp;nbsp; MRI scan is normal, cant quite believe it, the nightmare is over i have survived the most awful year but have come out the other side!!!!!!!!!!!!!!!!!!!!!!!!!!&lt;/p&gt;
&lt;p&gt;Would not of been able to do it without the support of my great family and friends&lt;/p&gt;
&lt;p&gt;To those who are still battling, keep the faith love to you all xxxxxxxxxxxxx&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=299929&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Survived" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/Survived" /><category term="MRI scan" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/MRI%2bscan" /></entry><entry><title>MRI</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/mri" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/mri</id><published>2009-11-26T09:16:28Z</published><updated>2009-11-26T09:16:28Z</updated><content type="html">&lt;p&gt;Yesterday i went for my MRI Jamie came with me so glad he did i would not of wanted to of gone on my own, it was strange walking down the corridor i remember it so clearly how scared i was nine months ago&lt;/p&gt;
&lt;p&gt;The lovely nurse lady remembered me and how she cried with me in February, she said how well i looked so thats always nice to hear!!, got changed into the sexy hospital gown then had a cannula put into the back of my hand, so brave lol. i did have a few tears&lt;/p&gt;
&lt;p&gt;so the MRI was fine took about 40 Min&amp;#39;s, trying to see if i can see concern in the ladies faces or hear it their voices but i have no idea what the results will be,&amp;nbsp;so now the wait begins,have no idea how long i will have to wait it was a week last time, Of course i get the what if&amp;#39;&amp;#39;s What if its come back can i do it all again and the honest truth is no but i know i will have too, On the flip side it could come back clear what an amazing Christmas present for me and my family!!&amp;nbsp; So all i have to do is not let the doubts in keep busy, what will be will be xxxxxxxxxxxxxxxxxxxx&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=276040&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="christmas" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/christmas" /><category term="Hospital" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/Hospital" /><category term="cannula" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/cannula" /></entry><entry><title>nervous</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/nervous" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/nervous</id><published>2009-11-24T11:04:39Z</published><updated>2009-11-24T11:04:39Z</updated><content type="html">&lt;p&gt;MRI tomorrow 25/11/09&amp;nbsp; and I&amp;#39;m nervous i feel fine but that don&amp;#39;t mean nothing, i pray it don&amp;#39;t show anything not sure if i can cope going through it again. i hope i don&amp;#39;t have to wait too long for results and i hope my legs carry me into that horrible little room to get the results, think its going to be a week of not much sleep and the dark little demons trying to sneak in and take over the positive thoughts.&lt;/p&gt;
&lt;p&gt;xxxxxxxxxxxxxxx&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=275388&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author></entry><entry><title>Positive news</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/positive-news" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/positive-news</id><published>2009-11-20T14:54:05Z</published><updated>2009-11-20T14:54:05Z</updated><content type="html">&lt;p&gt;It seems along time since i have had good news from the medical lot but today i had my cervix looked at for the first time since Feb and all looks good, still got to wait for the results but Mrs Gull was pleased with how it looked! What a relief&lt;/p&gt;
&lt;p&gt;So next&amp;nbsp;BIG test is MRI on Wednesday the 25th so fingers and anything else crossed!!&lt;/p&gt;
&lt;p&gt;xxxxxxxxxxxxxxxxxxxx&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=274159&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author></entry><entry><title>Prempak C</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/prempak-c" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/prempak-c</id><published>2009-11-16T15:17:50Z</published><updated>2009-11-16T15:17:50Z</updated><content type="html">&lt;p&gt;My Friday appointment went well, my consultant said i looked well and when i said i was in a new relationship she said i knew there was something different about you!!&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; But they have put me on HRT has im only 34 the likely hood of me getting osteoarthritis is high, but i read the side effects which i wish i had not!&amp;nbsp; but is there anyone who is on it with any words of advice Please&lt;/p&gt;
&lt;p&gt;xxxxx&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=272559&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Relationship" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/Relationship" /><category term="side effects" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/side%2beffects" /></entry><entry><title>Busy Bee</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/busy-bee" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/busy-bee</id><published>2009-11-12T07:31:07Z</published><updated>2009-11-12T07:31:07Z</updated><content type="html">&lt;p&gt;Well what a busy time of late, got a new tattoo and a new boyfriend all in the same week!!!&amp;nbsp; Tattoo three stars on my wrist symbolises me and my two boys, new boyfriend symbolises new adventure lol&lt;/p&gt;
&lt;p&gt;Something about him that makes me smile on the outside and within just what i needed!!&amp;nbsp;&amp;nbsp;&amp;nbsp; Got hospital appointment for tomorrow and he coming with me, he knows all about my cancer adventure and he still here amazing!!!&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/p&gt;
&lt;p&gt;xxx&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=271042&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Hospital" scheme="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/archive/tags/Hospital" /></entry><entry><title>I let myself feel sorry for me</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/i-let-myself-feel-sorry-for-me" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/i-let-myself-feel-sorry-for-me</id><published>2009-11-03T08:19:10Z</published><updated>2009-11-03T08:19:10Z</updated><content type="html">&lt;p&gt;Had a rough night last night, emotional, All this time i have tried to stay strong tell myself their are people worse off than me, But last night i did feel sorry for me and it felt ok to feel that way with out feeling guilty and this morning i feel a bit more at peace. xx&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=267793&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author></entry><entry><title>nice words</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/nice-words" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/nice-words</id><published>2009-11-02T07:31:10Z</published><updated>2009-11-02T07:31:10Z</updated><content type="html">&lt;p&gt;ur most devastating moments r actually your holliest, thats when u see who u really r. u can either breakdown or break open&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=267481&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author></entry><entry><title>Best day of my life!!</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/best-day-of-my-life" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/best-day-of-my-life</id><published>2009-10-25T16:45:02Z</published><updated>2009-10-25T16:45:02Z</updated><content type="html">&lt;p&gt;&lt;a href="http://community.macmillan.org.uk/cfs-file.ashx/__key/CommunityServer.Blogs.Components.WeblogFiles/emmaemily34/7215.004.JPG"&gt;&lt;img src="http://community.macmillan.org.uk/resized-image.ashx/__size/550x0/__key/CommunityServer.Blogs.Components.WeblogFiles/emmaemily34/7215.004.JPG" border="0" alt="" /&gt;&lt;/a&gt;Oh My Goodness, What a fantastic day!&lt;/p&gt;
&lt;p&gt;Was picked up in the most amazing car! had a tour of London, Big Ben,The Ritz,Buckingham Palace,China Town,Downing Street,London Eye &lt;/p&gt;
&lt;p&gt;Then it was time to be dropped of at the Hard Rock Caf&amp;eacute; had a lovely meal which we did not have to pay for, then the Limo picked us up and took us to see Grease which was fantastic!!!!!!!!&lt;/p&gt;
&lt;p&gt;It was simply the best day ever seeing my boys faces just taking it all in will stay with me forever and its a day they will remember for ever.&lt;/p&gt;
&lt;p&gt;AMAZING!!!!!&amp;nbsp;&amp;nbsp;&amp;nbsp; Tired today so we having a rest day with smiles on our faces&lt;/p&gt;
&lt;p&gt;xxxxxxxxxxx&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=262726&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author></entry><entry><title>My special day</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/my-special-day" /><id>https://community.macmillan.org.uk/cancer-blogs/b/emmaemily34/posts/my-special-day</id><published>2009-10-17T09:34:45Z</published><updated>2009-10-17T09:34:45Z</updated><content type="html">&lt;p&gt;Thanks to the Willow Foundation today i have a limousine coming to my house to pick me, my sister and my two lovely boys, its taking us to The Hard Rock Caf&amp;eacute; in London then to the Theater to watch Grease, I&amp;#39;m so excited!! what a wonderful treat.&lt;/p&gt;
&lt;p&gt;Will let you know how it goes, am going to try to raise the money so i can pay them back and make it possible for someone else to have a special day&lt;/p&gt;
&lt;p&gt;xxx&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=262454&amp;AppID=20556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author></entry></feed>